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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 2-189854273-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=189854273&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 189854273,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000441310.7",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "NM_000534.5",
"protein_id": "NP_000525.1",
"transcript_support_level": null,
"aa_start": 334,
"aa_end": null,
"aa_length": 932,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2799,
"cdna_start": 1165,
"cdna_end": null,
"cdna_length": 3156,
"mane_select": "ENST00000441310.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "ENST00000441310.7",
"protein_id": "ENSP00000406490.3",
"transcript_support_level": 1,
"aa_start": 334,
"aa_end": null,
"aa_length": 932,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2799,
"cdna_start": 1165,
"cdna_end": null,
"cdna_length": 3156,
"mane_select": "NM_000534.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.356C>T",
"hgvs_p": "p.Thr119Met",
"transcript": "ENST00000409593.5",
"protein_id": "ENSP00000387169.1",
"transcript_support_level": 1,
"aa_start": 119,
"aa_end": null,
"aa_length": 555,
"cds_start": 356,
"cds_end": null,
"cds_length": 1668,
"cdna_start": 356,
"cdna_end": null,
"cdna_length": 1668,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "n.884C>T",
"hgvs_p": null,
"transcript": "ENST00000424059.1",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2004,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "NM_001321045.2",
"protein_id": "NP_001307974.1",
"transcript_support_level": null,
"aa_start": 334,
"aa_end": null,
"aa_length": 932,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2799,
"cdna_start": 1291,
"cdna_end": null,
"cdna_length": 3282,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "NM_001321047.2",
"protein_id": "NP_001307976.1",
"transcript_support_level": null,
"aa_start": 334,
"aa_end": null,
"aa_length": 932,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2799,
"cdna_start": 1342,
"cdna_end": null,
"cdna_length": 3333,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "NM_001321048.2",
"protein_id": "NP_001307977.1",
"transcript_support_level": null,
"aa_start": 334,
"aa_end": null,
"aa_length": 932,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2799,
"cdna_start": 1262,
"cdna_end": null,
"cdna_length": 3253,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "NM_001128143.2",
"protein_id": "NP_001121615.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 893,
"cds_start": 884,
"cds_end": null,
"cds_length": 2682,
"cdna_start": 1048,
"cdna_end": null,
"cdna_length": 3039,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "ENST00000409823.7",
"protein_id": "ENSP00000387125.3",
"transcript_support_level": 5,
"aa_start": 295,
"aa_end": null,
"aa_length": 893,
"cds_start": 884,
"cds_end": null,
"cds_length": 2682,
"cdna_start": 997,
"cdna_end": null,
"cdna_length": 2795,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.818C>T",
"hgvs_p": "p.Thr273Met",
"transcript": "NM_001321046.2",
"protein_id": "NP_001307975.1",
"transcript_support_level": null,
"aa_start": 273,
"aa_end": null,
"aa_length": 871,
"cds_start": 818,
"cds_end": null,
"cds_length": 2616,
"cdna_start": 982,
"cdna_end": null,
"cdna_length": 2973,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "NM_001128144.2",
"protein_id": "NP_001121616.1",
"transcript_support_level": null,
"aa_start": 334,
"aa_end": null,
"aa_length": 770,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 1165,
"cdna_end": null,
"cdna_length": 2670,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.1001C>T",
"hgvs_p": "p.Thr334Met",
"transcript": "ENST00000447232.6",
"protein_id": "ENSP00000401064.2",
"transcript_support_level": 2,
"aa_start": 334,
"aa_end": null,
"aa_length": 770,
"cds_start": 1001,
"cds_end": null,
"cds_length": 2313,
"cdna_start": 1071,
"cdna_end": null,
"cdna_length": 2576,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.473C>T",
"hgvs_p": "p.Thr158Met",
"transcript": "NM_001289408.2",
"protein_id": "NP_001276337.1",
"transcript_support_level": null,
"aa_start": 158,
"aa_end": null,
"aa_length": 756,
"cds_start": 473,
"cds_end": null,
"cds_length": 2271,
"cdna_start": 1062,
"cdna_end": null,
"cdna_length": 3053,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.473C>T",
"hgvs_p": "p.Thr158Met",
"transcript": "NM_001289409.2",
"protein_id": "NP_001276338.1",
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"cds_start": 473,
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"cdna_start": 879,
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"biotype": null,
"feature": null
},
{
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"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.473C>T",
"hgvs_p": "p.Thr158Met",
"transcript": "ENST00000432292.7",
"protein_id": "ENSP00000398378.3",
"transcript_support_level": 2,
"aa_start": 158,
"aa_end": null,
"aa_length": 756,
"cds_start": 473,
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"cds_length": 2271,
"cdna_start": 1244,
"cdna_end": null,
"cdna_length": 3234,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.473C>T",
"hgvs_p": "p.Thr158Met",
"transcript": "ENST00000624204.3",
"protein_id": "ENSP00000485312.1",
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "NM_001321044.2",
"protein_id": "NP_001307973.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 731,
"cds_start": 884,
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"cdna_start": 1048,
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"cdna_length": 2553,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.818C>T",
"hgvs_p": "p.Thr273Met",
"transcript": "ENST00000424307.5",
"protein_id": "ENSP00000389938.1",
"transcript_support_level": 5,
"aa_start": 273,
"aa_end": null,
"aa_length": 710,
"cds_start": 818,
"cds_end": null,
"cds_length": 2133,
"cdna_start": 838,
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"cdna_length": 2153,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "ENST00000418224.7",
"protein_id": "ENSP00000404492.4",
"transcript_support_level": 5,
"aa_start": 295,
"aa_end": null,
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"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "XM_017004344.2",
"protein_id": "XP_016859833.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 893,
"cds_start": 884,
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"cdna_start": 1174,
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"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "XM_024452966.2",
"protein_id": "XP_024308734.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 893,
"cds_start": 884,
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"cds_length": 2682,
"cdna_start": 1069,
"cdna_end": null,
"cdna_length": 3060,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
"hgvs_p": "p.Thr295Met",
"transcript": "XM_024452967.2",
"protein_id": "XP_024308735.1",
"transcript_support_level": null,
"aa_start": 295,
"aa_end": null,
"aa_length": 893,
"cds_start": 884,
"cds_end": null,
"cds_length": 2682,
"cdna_start": 1019,
"cdna_end": null,
"cdna_length": 3010,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "T",
"aa_alt": "M",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PMS1",
"gene_hgnc_id": 9121,
"hgvs_c": "c.884C>T",
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}
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}